BLEPHAROPHIMOSIS SEQUENCE AND DENOVO BALANCED AUTOSOMAL TRANSLOCATION [46,XY,T(3-4)(Q23-P15.2)] - POSSIBLE ASSIGNMENT OF THE TRAIT TO 3Q23

被引:46
|
作者
FUKUSHIMA, Y
WAKUI, K
NISHIDA, T
UEOKA, Y
机构
[1] SAITAMA CHILDRENS MED CTR,DEPT CLIN LAB,IWATSUKI,SAITAMA 339,JAPAN
[2] SAITAMA CHILDRENS HOSP,DEPT OPHTHALMOL,IWATSUKI,SAITAMA 339,JAPAN
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1991年 / 40卷 / 04期
关键词
DENOVO 3Q/4P TRANSLOCATION; GENE LOCALIZATION; CLINICAL MANIFESTATIONS;
D O I
10.1002/ajmg.1320400423
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on a boy with the blepharophimosis sequence and de novo, apparently balanced reciprocal translocation between 3q23 and 4p15.2 [46,XY,t(3;4)(q23;p15.2)de novo]. Possible assignment of this autosomal dominant disorder is discussed. A 3q23 band is a more preferable gene locus of the blepharophimosis sequence, based on the comparison of clinical manifestations between 4p- and 3q-syndromes.
引用
收藏
页码:485 / 487
页数:3
相关论文
共 50 条
  • [1] BLEPHAROPHIMOSIS, PTOSIS, EPICANTHUS INVERSUS SYNDROME, A NEW CASE ASSOCIATED WITH DE-NOVO BALANCED AUTOSOMAL TRANSLOCATION [46,XY,T(37) (Q23Q32)]
    BOCCONE, L
    MELONI, A
    FALCHI, AM
    USAI, V
    CAO, A
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 51 (03): : 258 - 259
  • [2] Blepharophimosis, ptosis, epicanthus inversus syndrome with translocation and deletion at chromosome 3q23 in a black African female
    Alao, M. J.
    Laleye, A.
    Lalya, F.
    Hans, Ch.
    Abramovicz, M.
    Morice-Picard, F.
    Arveiler, B.
    Lacombe, D.
    Rooryck, C.
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2012, 55 (11) : 630 - 634
  • [3] BLEPHAROPHIMOSIS SEQUENCE AND DIAPHRAGMATIC-HERNIA ASSOCIATED WITH INTERSTITIAL DELETION OF CHROMOSOME-3 (46,XY,DEL(3)(Q21Q23))
    WOLSTENHOLME, J
    BROWN, J
    MASTERS, KG
    WRIGHT, C
    ENGLISH, CJ
    JOURNAL OF MEDICAL GENETICS, 1994, 31 (08) : 647 - 648
  • [4] TRISOMY-3 (P23-PTER) RESULTING FROM MATERNAL TRANSLOCATION, T (3-4) (P23-Q35)
    SCHINZEL, A
    HANSON, JW
    PAGON, RA
    HOEHN, H
    SMITH, DW
    ANNALES DE GENETIQUE, 1978, 21 (03): : 168 - 171
  • [5] TRISOMY-3Q2 AND PIERRE-ROBIN SEQUENCE IN A BOY WITH UNBALANCED 46,XY, DER(10), T(3-10)(Q23-Q26.3) DENOVO KARYOTYPE
    KLECZKOWSKA, A
    FRYNS, JP
    MOERMAN, F
    MARTENS, M
    EGGERMONT, E
    JAEKEN, J
    VANDENBERGHE, H
    HELVETICA PAEDIATRICA ACTA, 1988, 43 (03) : 245 - 248
  • [6] Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPES
    De Baere, E
    Fukushima, Y
    Small, K
    Udar, N
    Van Camp, G
    Verhoeven, K
    Palotie, A
    De Paepe, A
    Messiaen, L
    GENOMICS, 2000, 68 (03) : 296 - 304
  • [7] Microdeletion found by array-CGH in girl with Blepharophimosis syndrome and apparently balanced translocation t(3;15)(q23;q25)
    Gonzalez-Gonzalez, Cristina
    Garcia-Hoyos, Maria
    Hernaez Calzon, Rosario
    Arroyo Diaz, Carolina
    Gonzalez Fanego, Cristina
    Lorda Sanchez, Isabel
    Sanchez-Escribano, Fernando
    OPHTHALMIC GENETICS, 2012, 33 (02) : 107 - 110
  • [8] 一例46,XY,del(3),t(3;7)(q23;q33)
    于秀琴
    么桂芳
    靳耀英
    中华医学遗传学杂志, 1992, (01) : 50 - 50
  • [9] 46,XY,t(3;21)(p23;q22)一例
    徐清华
    赵庆国
    朱爱萍
    张建萍
    中华医学遗传学杂志, 1999, (04) : 63 - 63
  • [10] 46,XY,T(3-17)(P14-Q23) - NEW CHROMOSOME ABERRATION
    CLARK, CE
    TELFER, MA
    PAULSON, KM
    AMERICAN JOURNAL OF HUMAN GENETICS, 1978, 30 (06) : A76 - A76